HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911651Generated: October 30, 2026
Cycloheptanol → 4-(Cycloheptyloxy)benzonitrile
https://huagongshe.com/reaction/911651
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cycloheptanol | HCID 10399 | — |
| Reactant | 4-Cyanophenol | HCID 13019 | — |
| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | Azodicarboxylate dipiperidine | HCID 66707187 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(Cycloheptyloxy)benzonitrile | HCID 57656625 | 58% |
Reaction Steps
Under a nitrogen atmosphere, add 4-hydroxybenzonitrile (4 g, 33.5 mmol), cycloheptanol (2.55 g, 22.3 mmol), tri-n-butylphosphine (8.25 mL, 33.5 mmol), and azodicarboxylate dipiperidine (8.45 g, 33.5 mmol) to anhydrous THF (60 mL) at 0° C. Stir the mixture at 0° C. for 1 h and then at room temperature for 12 h. Dilute with EtOAc (50 mL) and water (50 mL). Separate the layers and extract the aqueous phase with EtOAc (4×30 mL). Wash the combined organic extracts with water (30 mL) and brine (20 mL). Dry over Na2SO4, filter and concentrate in vacuo. Purify the crude mixture by chromatography on silica gel (120 g RediSep column) eluting with hexane/EtOAc (1:0 to 1:1 gradient over 1.25 h; 80 mL/min) to provide the desired intermediate as a colorless oil (2.77 g, 58%). MS (APCI) m/z: 216 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022062B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-f222f151b4c24039887e27f997028623 |
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| Source note | uspto-grants-2011_09 |
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